Canonical Allele Identifier: PA204871
Gene: TBX6 HGNC NCBI

Linked Data

ClinVar Variation Id: 208772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004599.2:p.Arg171His
CA204870
NM_004608.4:c.512G>A